A new series of 2-substituted 3-phosphonic derivatives of chromone. Part II. Synthesis, in vitro alkylating and in vivo antitumour activity

New Journal of Chemistry

Volumn 26, Issue 12, 2002, Pages 1799-1804

  Budzisz, Elzbieta ^a   Graczyk Wojciechowska, Julita ^a   Zieba, Remigiusz ^a   Nawrot, Barbara ^b  

^a MEDICAL UNIVERSITY OF LODZ   (Poland)

^b CENTRE OF MOLECULAR AND MACROMOLECULAR STUDIES   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

(4 OXO 3 PHOSPHONO 4H CHROMEN 2 YL)PHENYLMETHYL ACETATE; (4 OXO 4H CHROMEN 2 YL)PHENYLMETHYL ACETATE; (6 METHYL 4 OXO 3 PHOSPHONO 4H CHROMEN 2 YL)PHENYLMETHYL ACETATE; (6 METHYL 4 OXO 4H CHROMEN 2 YL)PHENYLMETHYL ACETATE; 1 HYDROXY 1 OXO 3 3 PHENYL 1,3 DIHYDRO 1LAMBDA 5 2,1 OXAPHOSPHOLO[4,5 B] 4H 1 BENZOPYRAN 4 ON; 1 HYDROXY 1 OXO 3 PHENYL 1,3 DIHYDRO 1LAMBDA 5 2,1 OXAPHOSPHOLO[4,5 B] 4H 1 BENZOPYRAN 4 ONE; 1 HYDROXY 7 METHYL 1 OXO 3 3 PHENYL 1,3 DIHYDRO 1LAMBDA 5 2,1 OXAPHOSPHOLO[4,5 B] 4H 1 BENZOPYRAN 4 ONE BENZYLAMMONIUM DERIVATIVE; 1 HYDROXY 7 METHYL 1 OXO 3 PHENYL 1,3 DIHYDRO 1LAMBDA 5 2,1 OXAPHOSPHOLO[4,5 B] 4H 1 BENZOPYRAN 4 ONE; 2 (1 ACETOXYBENZYL) 3 (DIMETHOXYPHOSPHORYL) 4 OXO 4H CHROMENE; 2 (1 ACETOXYBENZYL) 3 (DIMETHOXYPHOSPHORYL) 6 METHYL 4 OXO 4H CHROMENE; 2 HYDROXY 5 METHYLACETOPHENONE; ACETIC ACID DERIVATIVE; ACETOPHENONE DERIVATIVE; ACETOXYPHENYLACETIC ACID 2 [1 (DIMETHOXYPHOSPHORYLOXY)VINYL] 4 METHYLPHENYL ESTER; ACETOXYPHENYLACETIC ACID 2 [1 (DIMETHOXYPHOSPHORYLOXY)VINYL]PHENYL ESTER; AMMONIUM DERIVATIVE; BROMINE; CHEMICAL COMPOUND; CHLORIDE; CHROMONE DERIVATIVE; ESTER DERIVATIVE; O ACETYLMANDELOYL CHLORIDE; PHOSPHITE; PHOSPHONIC ACID DERIVATIVE; PYRAN DERIVATIVE; TRIMETHYL PHOSPHITE; UNCLASSIFIED DRUG;

ALKYLATION; ANTINEOPLASTIC ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; IN VITRO STUDY; IN VIVO STUDY; LABORATORY TEST; LYMPHATIC LEUKEMIA; MASS SPECTROMETRY; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SPECTROMETRY; SYNTHESIS; ULTRAVIOLET RADIATION; WITTIG REACTION;

EID: 0036446027     PISSN: 11440546     EISSN: None     Source Type: Journal    
DOI: 10.1039/b205800f     Document Type: Article

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